Canonical Allele Identifier: CA8255604
Gene: MC1R HGNC NCBI

Linked Data

dbSNP Id: rs756422682

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919727A>C , CM000678.2:g.89919727A>C GRCh38
NC_000016.9:g.89986135A>C , CM000678.1:g.89986135A>C GRCh37
NC_000016.8:g.88513636A>C NCBI36
NG_012026.1:g.6849A>C
NG_027810.1:g.2719A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.469A>C MANE Select ENSP00000451605.1:p.Thr157Pro
ENST00000639847.1:c.469A>C ENSP00000492011.1:p.Thr157Pro
ENST00000555147.1:c.469A>C ENSP00000451605.1:p.Thr157Pro
ENST00000555427.1:c.469A>C ENSP00000451760.1:p.Thr157Pro
ENST00000556922.1:c.469A>C ENSP00000451560.1:p.Thr157Pro
NM_002386.3:c.469A>C NP_002377.4:p.Thr157Pro
NM_002386.4:c.469A>C MANE Select NP_002377.4:p.Thr157Pro